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Proteins in Complement, Immune, and Clotting Cascades and their Role in Preterm Births
Shubham Thakur1, Subheet Kumar Jain1,2
1Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, 143005, India.
Insights
Preterm birth (PTB) is a major cause of infant mortality. Research suggests imbalances in complement, immune, and clotting cascade proteins may predict PTB, aiding early detection.
Area of Science:
- Obstetrics and Gynecology
- Immunology
- Hematology
Background:
- Preterm birth (PTB) is a significant global health concern, leading to infant mortality and long-term developmental issues.
- The exact mechanisms underlying PTB remain incompletely understood, necessitating further research into potential contributing factors.
- Certain protein pathways, including the complement cascade, immune system, and clotting cascade, are implicated in PTB etiology.
Conclusions:
- Circulating proteins, particularly those in the complement, immune, and clotting cascades, are critical factors in PTB.
- Further investigation into these proteins can enhance the understanding of PTB mechanisms and facilitate early identification.
- Targeting research on these protein pathways holds promise for developing novel biomarkers and interventions for PTB.
Abstract:
Preterm birth (PTB) (< 37 completed weeks gestation) is a pathological outcome of pregnancy and its associated complications are the leading global cause of death in children younger than 5 years of age. Babies born prematurely have an elevated risk for short- and long-term adverse effects of medical and neurodevelopmental sequelae. Substantial evidence suggests that multiple sets of symptoms are allied with PTB etiology, and the exact mechanism cannot be recognized. Notably, various proteins, especially (i) complement cascade; (ii) immune system; and (iii) clotting cascade, have become attractive research targets that are associated with PTB. Further, a small imbalance of these proteins in maternal or foetal circulation could serve as a marker/precursor in a series of events that lead to PTBs. Thus, the present review lightens the basic description of the circulating proteins, their role in PTB, and current concepts for future development. Further, deepening the research on these proteins will lead to a better understanding of PTB etiology and alleviate scientists' confidence in the early identification of PTB mechanisms and biological markers.
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